Hepatitis Associated Aplastic Anemia: A review

<p>Abstract</p> <p>Hepatitis-associated aplastic anemia (HAAA) is an uncommon but distinct variant of aplastic anemia in which pancytopenia appears two to three months after an acute attack of hepatitis. HAAA occurs most frequently in young male children and is lethal if leave untr...

Full description

Bibliographic Details
Main Authors: Irshad-ur-Rehman, Hussain Abrar, Ali Liaqat, Butt Azeem M, Butt Sadia, Shah Shahida, Idrees Muhammad, Rauff Bisma, Ali Muhammad
Format: Article
Language:English
Published: BMC 2011-02-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/8/1/87
id doaj-cb32048f840e46bcacecea8dad1044c2
record_format Article
spelling doaj-cb32048f840e46bcacecea8dad1044c22020-11-25T00:24:59ZengBMCVirology Journal1743-422X2011-02-01818710.1186/1743-422X-8-87Hepatitis Associated Aplastic Anemia: A reviewIrshad-ur-RehmanHussain AbrarAli LiaqatButt Azeem MButt SadiaShah ShahidaIdrees MuhammadRauff BismaAli Muhammad<p>Abstract</p> <p>Hepatitis-associated aplastic anemia (HAAA) is an uncommon but distinct variant of aplastic anemia in which pancytopenia appears two to three months after an acute attack of hepatitis. HAAA occurs most frequently in young male children and is lethal if leave untreated. The etiology of this syndrome is proposed to be attributed to various hepatitis and non hepatitis viruses. Several hepatitis viruses such as HAV, HBV, HCV, HDV, HEV and HGV have been associated with this set of symptoms. Viruses other than the hepatitis viruses such as parvovirus B19, Cytomegalovirus, Epstein bar virus, Transfusion Transmitted virus (TTV) and non-A-E hepatitis virus (unknown viruses) has also been documented to develop the syndrome. Considerable evidences including the clinical features, severe imbalance of the T cell immune system and effective response to immunosuppressive therapy strongly present HAAA as an immune mediated mechanism. However, no association of HAAA has been found with blood transfusions, drugs and toxins. Besides hepatitis and non hepatitis viruses and immunopathogenesis phenomenon as causative agents of the disorder, telomerase mutation, a genetic factor has also been predisposed for the development of aplastic anemia. Diagnosis includes clinical manifestations, blood profiling, viral serological markers testing, immune functioning and bone marrow hypocellularity examination. Patients presenting the features of HAAA have been mostly treated with bone marrow or hematopoietic cell transplantation from HLA matched donor, and if not available then by immunosuppressive therapy. New therapeutic approaches involve the administration of steroids especially the glucocorticoids to augment the immunosuppressive therapy response. Pancytopenia following an episode of acute hepatitis response better to hematopoietic cell transplantation than immunosuppressive therapy.</p> http://www.virologyj.com/content/8/1/87
collection DOAJ
language English
format Article
sources DOAJ
author Irshad-ur-Rehman
Hussain Abrar
Ali Liaqat
Butt Azeem M
Butt Sadia
Shah Shahida
Idrees Muhammad
Rauff Bisma
Ali Muhammad
spellingShingle Irshad-ur-Rehman
Hussain Abrar
Ali Liaqat
Butt Azeem M
Butt Sadia
Shah Shahida
Idrees Muhammad
Rauff Bisma
Ali Muhammad
Hepatitis Associated Aplastic Anemia: A review
Virology Journal
author_facet Irshad-ur-Rehman
Hussain Abrar
Ali Liaqat
Butt Azeem M
Butt Sadia
Shah Shahida
Idrees Muhammad
Rauff Bisma
Ali Muhammad
author_sort Irshad-ur-Rehman
title Hepatitis Associated Aplastic Anemia: A review
title_short Hepatitis Associated Aplastic Anemia: A review
title_full Hepatitis Associated Aplastic Anemia: A review
title_fullStr Hepatitis Associated Aplastic Anemia: A review
title_full_unstemmed Hepatitis Associated Aplastic Anemia: A review
title_sort hepatitis associated aplastic anemia: a review
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-02-01
description <p>Abstract</p> <p>Hepatitis-associated aplastic anemia (HAAA) is an uncommon but distinct variant of aplastic anemia in which pancytopenia appears two to three months after an acute attack of hepatitis. HAAA occurs most frequently in young male children and is lethal if leave untreated. The etiology of this syndrome is proposed to be attributed to various hepatitis and non hepatitis viruses. Several hepatitis viruses such as HAV, HBV, HCV, HDV, HEV and HGV have been associated with this set of symptoms. Viruses other than the hepatitis viruses such as parvovirus B19, Cytomegalovirus, Epstein bar virus, Transfusion Transmitted virus (TTV) and non-A-E hepatitis virus (unknown viruses) has also been documented to develop the syndrome. Considerable evidences including the clinical features, severe imbalance of the T cell immune system and effective response to immunosuppressive therapy strongly present HAAA as an immune mediated mechanism. However, no association of HAAA has been found with blood transfusions, drugs and toxins. Besides hepatitis and non hepatitis viruses and immunopathogenesis phenomenon as causative agents of the disorder, telomerase mutation, a genetic factor has also been predisposed for the development of aplastic anemia. Diagnosis includes clinical manifestations, blood profiling, viral serological markers testing, immune functioning and bone marrow hypocellularity examination. Patients presenting the features of HAAA have been mostly treated with bone marrow or hematopoietic cell transplantation from HLA matched donor, and if not available then by immunosuppressive therapy. New therapeutic approaches involve the administration of steroids especially the glucocorticoids to augment the immunosuppressive therapy response. Pancytopenia following an episode of acute hepatitis response better to hematopoietic cell transplantation than immunosuppressive therapy.</p>
url http://www.virologyj.com/content/8/1/87
work_keys_str_mv AT irshadurrehman hepatitisassociatedaplasticanemiaareview
AT hussainabrar hepatitisassociatedaplasticanemiaareview
AT aliliaqat hepatitisassociatedaplasticanemiaareview
AT buttazeemm hepatitisassociatedaplasticanemiaareview
AT buttsadia hepatitisassociatedaplasticanemiaareview
AT shahshahida hepatitisassociatedaplasticanemiaareview
AT idreesmuhammad hepatitisassociatedaplasticanemiaareview
AT rauffbisma hepatitisassociatedaplasticanemiaareview
AT alimuhammad hepatitisassociatedaplasticanemiaareview
_version_ 1725350501859459072